Chloe's Fight has only been around since 2011, but is already considered the go-to organization in Minnesota for rare disease research support and advocacy. Chloe's Fight is passionately led by Erica and Philip Barnes, parents of Chloe Barnes who passed away from metachromatic leukodystrophy in 2010. I began working with CFF last year when I became aware of the promise current genetic disease research has, yet the lack of funding and attention it receives. Chloe's Fight is a small, but dedicated organization making a real difference in fighting rare genetic diseases. Thank you for your support!